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Open Access Research article

Short-term genome evolution of Listeria monocytogenes in a non-controlled environment

Renato H Orsi1, Mark L Borowsky27, Peter Lauer3, Sarah K Young2, Chad Nusbaum2, James E Galagan24, Bruce W Birren2, Reid A Ivy1, Qi Sun5, Lewis M Graves6, Bala Swaminathan6 and Martin Wiedmann1*

Author Affiliations

1 Department of Food Science, Cornell University, Ithaca, USA

2 Genome Sequencing and Analysis Program, Broad Institute of MIT and Harvard, Cambridge, USA

3 Anza Therapeutics, Concord, USA

4 Department of Biomedical Engineering and Microbiology, Boston University, USA

5 Computational Biology Services Unit, Center for Advanced Computing, Cornell University, Ithaca, USA

6 Enteric Diseases Laboratory Branch, Division of Foodborne, Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, USA

7 Department of Molecular Biology, Massachusetts General Hospital, Boston, USA

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BMC Genomics 2008, 9:539  doi:10.1186/1471-2164-9-539

Published: 13 November 2008

Abstract

Background

While increasing data on bacterial evolution in controlled environments are available, our understanding of bacterial genome evolution in natural environments is limited. We thus performed full genome analyses on four Listeria monocytogenes, including human and food isolates from both a 1988 case of sporadic listeriosis and a 2000 listeriosis outbreak, which had been linked to contaminated food from a single processing facility. All four isolates had been shown to have identical subtypes, suggesting that a specific L. monocytogenes strain persisted in this processing plant over at least 12 years. While a genome sequence for the 1988 food isolate has been reported, we sequenced the genomes of the 1988 human isolate as well as a human and a food isolate from the 2000 outbreak to allow for comparative genome analyses.

Results

The two L. monocytogenes isolates from 1988 and the two isolates from 2000 had highly similar genome backbone sequences with very few single nucleotide (nt) polymorphisms (1 – 8 SNPs/isolate; confirmed by re-sequencing). While no genome rearrangements were identified in the backbone genome of the four isolates, a 42 kb prophage inserted in the chromosomal comK gene showed evidence for major genome rearrangements. The human-food isolate pair from each 1988 and 2000 had identical prophage sequence; however, there were significant differences in the prophage sequences between the 1988 and 2000 isolates. Diversification of this prophage appears to have been caused by multiple homologous recombination events or possibly prophage replacement. In addition, only the 2000 human isolate contained a plasmid, suggesting plasmid loss or acquisition events. Surprisingly, besides the polymorphisms found in the comK prophage, a single SNP in the tRNA Thr-4 prophage represents the only SNP that differentiates the 1988 isolates from the 2000 isolates.

Conclusion

Our data support the hypothesis that the 2000 human listeriosis outbreak was caused by a L. monocytogenes strain that persisted in a food processing facility over 12 years and show that genome sequencing is a valuable and feasible tool for retrospective epidemiological analyses. Short-term evolution of L. monocytogenes in non-controlled environments appears to involve limited diversification beyond plasmid gain or loss and prophage diversification, highlighting the importance of phages in bacterial evolution.